CA2741736A1 - Epoxide-based structural foam having improved tenacity - Google Patents
Epoxide-based structural foam having improved tenacity Download PDFInfo
- Publication number
- CA2741736A1 CA2741736A1 CA2741736A CA2741736A CA2741736A1 CA 2741736 A1 CA2741736 A1 CA 2741736A1 CA 2741736 A CA2741736 A CA 2741736A CA 2741736 A CA2741736 A CA 2741736A CA 2741736 A1 CA2741736 A1 CA 2741736A1
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- CA
- Canada
- Prior art keywords
- thermally expandable
- curable compound
- compound according
- block
- shell
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
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- 150000002118 epoxides Chemical class 0.000 title claims abstract description 5
- 239000004616 structural foam Substances 0.000 title description 9
- 239000004433 Thermoplastic polyurethane Substances 0.000 claims abstract description 30
- 229920002803 thermoplastic polyurethane Polymers 0.000 claims abstract description 30
- 229920001400 block copolymer Polymers 0.000 claims abstract description 27
- 239000012948 isocyanate Substances 0.000 claims abstract description 9
- 150000002513 isocyanates Chemical class 0.000 claims abstract description 9
- 150000001875 compounds Chemical class 0.000 claims description 40
- 239000002245 particle Substances 0.000 claims description 31
- 239000000126 substance Substances 0.000 claims description 31
- 229920000642 polymer Polymers 0.000 claims description 28
- 229920001971 elastomer Polymers 0.000 claims description 18
- 239000010954 inorganic particle Substances 0.000 claims description 18
- 239000004604 Blowing Agent Substances 0.000 claims description 17
- 229920000620 organic polymer Polymers 0.000 claims description 17
- 239000011258 core-shell material Substances 0.000 claims description 16
- 239000005060 rubber Substances 0.000 claims description 16
- 239000000945 filler Substances 0.000 claims description 15
- 229920001577 copolymer Polymers 0.000 claims description 14
- 229920000728 polyester Polymers 0.000 claims description 14
- 239000007787 solid Substances 0.000 claims description 14
- 230000009477 glass transition Effects 0.000 claims description 13
- 239000000835 fiber Substances 0.000 claims description 12
- 229920002635 polyurethane Polymers 0.000 claims description 11
- 239000004814 polyurethane Substances 0.000 claims description 11
- 238000002844 melting Methods 0.000 claims description 7
- 230000008018 melting Effects 0.000 claims description 7
- 239000005062 Polybutadiene Substances 0.000 claims description 5
- 239000004793 Polystyrene Substances 0.000 claims description 5
- 229920003229 poly(methyl methacrylate) Polymers 0.000 claims description 5
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- 239000004926 polymethyl methacrylate Substances 0.000 claims description 5
- 229920002223 polystyrene Polymers 0.000 claims description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 3
- 229920001195 polyisoprene Polymers 0.000 claims description 3
- IBARAOFMHIVQQI-UHFFFAOYSA-N butyl prop-2-enoate;methyl 2-methylprop-2-enoate Chemical compound COC(=O)C(C)=C.COC(=O)C(C)=C.CCCCOC(=O)C=C IBARAOFMHIVQQI-UHFFFAOYSA-N 0.000 claims description 2
- 230000002787 reinforcement Effects 0.000 claims description 2
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- 239000000463 material Substances 0.000 abstract description 20
- 239000003795 chemical substances by application Substances 0.000 abstract description 18
- 230000003014 reinforcing effect Effects 0.000 abstract description 8
- 239000004088 foaming agent Substances 0.000 abstract 1
- 229920000647 polyepoxide Polymers 0.000 description 41
- 239000003822 epoxy resin Substances 0.000 description 38
- 239000000203 mixture Substances 0.000 description 31
- -1 e.g. Substances 0.000 description 29
- 239000011257 shell material Substances 0.000 description 26
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 22
- 239000004593 Epoxy Substances 0.000 description 17
- 238000004519 manufacturing process Methods 0.000 description 17
- 238000001746 injection moulding Methods 0.000 description 16
- 239000000178 monomer Substances 0.000 description 15
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 13
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- 239000002184 metal Substances 0.000 description 13
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- 238000000034 method Methods 0.000 description 11
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 9
- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 9
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical class C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 9
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- 239000011324 bead Substances 0.000 description 8
- 238000006243 chemical reaction Methods 0.000 description 8
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 7
- 238000007906 compression Methods 0.000 description 7
- 230000006835 compression Effects 0.000 description 7
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 6
- KUBDPQJOLOUJRM-UHFFFAOYSA-N 2-(chloromethyl)oxirane;4-[2-(4-hydroxyphenyl)propan-2-yl]phenol Chemical compound ClCC1CO1.C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 KUBDPQJOLOUJRM-UHFFFAOYSA-N 0.000 description 5
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 5
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 5
- 125000005396 acrylic acid ester group Chemical group 0.000 description 5
- 125000001931 aliphatic group Chemical group 0.000 description 5
- 125000003118 aryl group Chemical group 0.000 description 5
- 239000007795 chemical reaction product Substances 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
- 150000002170 ethers Chemical class 0.000 description 5
- 238000001125 extrusion Methods 0.000 description 5
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- 125000005397 methacrylic acid ester group Chemical group 0.000 description 5
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- 238000006116 polymerization reaction Methods 0.000 description 5
- 230000008569 process Effects 0.000 description 5
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 4
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 4
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- 229920000459 Nitrile rubber Polymers 0.000 description 4
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 230000004913 activation Effects 0.000 description 4
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 4
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 description 4
- 238000005187 foaming Methods 0.000 description 4
- 239000011325 microbead Substances 0.000 description 4
- 239000000377 silicon dioxide Substances 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- 239000004721 Polyphenylene oxide Substances 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 239000011230 binding agent Substances 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 238000013016 damping Methods 0.000 description 3
- 239000003085 diluting agent Substances 0.000 description 3
- 150000002009 diols Chemical class 0.000 description 3
- 125000003700 epoxy group Chemical group 0.000 description 3
- XXOYNJXVWVNOOJ-UHFFFAOYSA-N fenuron Chemical compound CN(C)C(=O)NC1=CC=CC=C1 XXOYNJXVWVNOOJ-UHFFFAOYSA-N 0.000 description 3
- 239000006260 foam Substances 0.000 description 3
- 150000002357 guanidines Chemical class 0.000 description 3
- 150000004679 hydroxides Chemical class 0.000 description 3
- 239000011159 matrix material Substances 0.000 description 3
- 150000002739 metals Chemical class 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
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- 229920000570 polyether Polymers 0.000 description 3
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- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 3
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
- XMTQQYYKAHVGBJ-UHFFFAOYSA-N 3-(3,4-DICHLOROPHENYL)-1,1-DIMETHYLUREA Chemical compound CN(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 XMTQQYYKAHVGBJ-UHFFFAOYSA-N 0.000 description 2
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 2
- XAYDWGMOPRHLEP-UHFFFAOYSA-N 6-ethenyl-7-oxabicyclo[4.1.0]heptane Chemical compound C1CCCC2OC21C=C XAYDWGMOPRHLEP-UHFFFAOYSA-N 0.000 description 2
- GZVHEAJQGPRDLQ-UHFFFAOYSA-N 6-phenyl-1,3,5-triazine-2,4-diamine Chemical class NC1=NC(N)=NC(C=2C=CC=CC=2)=N1 GZVHEAJQGPRDLQ-UHFFFAOYSA-N 0.000 description 2
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- CTKINSOISVBQLD-UHFFFAOYSA-N Glycidol Chemical compound OCC1CO1 CTKINSOISVBQLD-UHFFFAOYSA-N 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
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- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
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- 125000000623 heterocyclic group Chemical group 0.000 description 2
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- CHJJGSNFBQVOTG-UHFFFAOYSA-N methylguanidine Chemical compound CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 description 2
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- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
- NBNGHXWJFSMASY-UHFFFAOYSA-N 2,3,4-tris(dimethylamino)phenol Chemical compound CN(C)C1=CC=C(O)C(N(C)C)=C1N(C)C NBNGHXWJFSMASY-UHFFFAOYSA-N 0.000 description 1
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- HHRACYLRBOUBKM-UHFFFAOYSA-N 2-[(4-tert-butylphenoxy)methyl]oxirane Chemical compound C1=CC(C(C)(C)C)=CC=C1OCC1OC1 HHRACYLRBOUBKM-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- C08J9/0066—Use of inorganic compounding ingredients
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/04—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
- C08G59/4007—Curing agents not provided for by the groups C08G59/42 - C08G59/66
- C08G59/4014—Nitrogen containing compounds
- C08G59/4021—Ureas; Thioureas; Guanidines; Dicyandiamides
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/0061—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof characterized by the use of several polymeric components
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L53/00—Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
- C08L75/04—Polyurethanes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2201/00—Foams characterised by the foaming process
- C08J2201/02—Foams characterised by the foaming process characterised by mechanical pre- or post-treatments
- C08J2201/024—Preparation or use of a blowing agent concentrate, i.e. masterbatch in a foamable composition
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2363/00—Characterised by the use of epoxy resins; Derivatives of epoxy resins
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2453/00—Characterised by the use of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2475/00—Characterised by the use of polyureas or polyurethanes; Derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2203/00—Applications
- C08L2203/14—Applications used for foams
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/03—Polymer mixtures characterised by other features containing three or more polymers in a blend
- C08L2205/035—Polymer mixtures characterised by other features containing three or more polymers in a blend containing four or more polymers in a blend
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L53/00—Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
- C08L53/02—Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers of vinyl-aromatic monomers and conjugated dienes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
- C08L75/04—Polyurethanes
- C08L75/06—Polyurethanes from polyesters
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Inorganic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
- Epoxy Resins (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102008053518A DE102008053518A1 (de) | 2008-10-28 | 2008-10-28 | Epoxid-basierter Strukturschaum mit verbesserter Zähigkeit |
| DE102008053518.4 | 2008-10-28 | ||
| PCT/EP2009/062310 WO2010049220A1 (de) | 2008-10-28 | 2009-09-23 | Epoxid-basierter strukturschaum mit verbesserter zähigkeit |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2741736A1 true CA2741736A1 (en) | 2010-05-06 |
Family
ID=41327272
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA2741736A Abandoned CA2741736A1 (en) | 2008-10-28 | 2009-09-23 | Epoxide-based structural foam having improved tenacity |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US20110257285A1 (de) |
| EP (1) | EP2350177B1 (de) |
| JP (1) | JP2012506918A (de) |
| KR (1) | KR20110079687A (de) |
| CN (1) | CN102197070B (de) |
| BR (1) | BRPI0920077A2 (de) |
| CA (1) | CA2741736A1 (de) |
| DE (1) | DE102008053518A1 (de) |
| ES (1) | ES2402757T3 (de) |
| WO (1) | WO2010049220A1 (de) |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102009026548A1 (de) | 2009-05-28 | 2011-03-24 | Henkel Ag & Co. Kgaa | Klebefolie oder Klebeband auf Basis von Epoxiden |
| DE102009046157A1 (de) * | 2009-10-29 | 2011-05-05 | Henkel Ag & Co. Kgaa | Vormischung und Verfahren zur Herstellung einer thermisch expandierbaren und härtbaren Epoxid-basierten Masse |
| DE102011080223A1 (de) | 2011-08-01 | 2013-02-07 | Henkel Ag & Co. Kgaa | Thermisch härtbare Zubereitungen |
| ITMI20120135A1 (it) * | 2012-02-02 | 2013-08-03 | Diab Int Ab | Procedimento per la produzione di schiume di pet e schiume di pet ottenute con questo procedimento |
| GB201201885D0 (en) * | 2012-02-03 | 2012-03-21 | Knauf Insulation Doo Skofa Loka | Composite fibre panel |
| EP2819193B1 (de) * | 2012-02-24 | 2016-09-28 | Kyushu Institute of Technology | Thermoelektrisches umwandlungsmaterial |
| BR112014032402A2 (pt) | 2012-06-28 | 2017-06-27 | Henkel Ag & Co Kgaa | método de produção de um inserto composto |
| DE102012221192A1 (de) * | 2012-11-20 | 2014-05-22 | Henkel Ag & Co. Kgaa | Thermisch expandierbare Zubereitungen |
| ES2718374T3 (es) * | 2013-11-20 | 2019-07-01 | Basf Se | Artículos celulares de poliuretano termoplástico que comprenden una composición de poliuretano termoplástico y un copolímero de estireno-acrílico con funcionalidad epoxi |
| US9390858B2 (en) * | 2014-04-03 | 2016-07-12 | Murata Manufacturing Co., Ltd. | Electronic component, method of manufacturing the same, and mount structure of electronic component |
| DE102014221060A1 (de) | 2014-10-16 | 2016-04-21 | Henkel Ag & Co. Kgaa | Thermisch expandierbare Zusammensetzung |
| FR3043682B1 (fr) * | 2015-11-16 | 2019-06-21 | Arkema France | Composition polymere comprenant un materiau vegetal disperse |
| CN107501974A (zh) * | 2017-09-02 | 2017-12-22 | 安徽金睐格环保科技有限公司 | 一种环保型阻燃耐热的包装箱板 |
| CN109161186A (zh) * | 2018-08-21 | 2019-01-08 | 瑞安市鸿日塑胶有限公司 | 一种防水tpu薄膜工艺和配方 |
| US20220010175A1 (en) * | 2018-11-05 | 2022-01-13 | Zephyros, Inc. | Single Layer Self-Adhering Reinforcing Patch |
| GB2582919B (en) * | 2019-04-05 | 2022-07-13 | Henkel IP & Holding GmbH | Anaerobically curable compositions |
| EP4001352B1 (de) * | 2020-11-11 | 2025-09-17 | Sika Technology AG | Expandierbares material mit verbesserten wärmedämmeigenschaften und dessen verwendung |
| EP4698575A1 (de) * | 2023-04-20 | 2026-02-25 | PRC-Desoto International, Inc. | Syntaktische schaumzusammensetzungen |
Family Cites Families (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3897586A (en) * | 1970-08-05 | 1975-07-29 | Du Pont | Polymer coated pigment particles and a process for their preparation |
| GB1430922A (en) * | 1973-02-03 | 1976-04-07 | Lion Fat Oil Co Ltd | Processes for coating aprticles of inorganic substances with polymeric materials |
| US4258137A (en) * | 1979-10-11 | 1981-03-24 | W. R. Grace & Co. | Rigidized open cell polyurethane foam |
| JPS5734151A (en) * | 1980-08-11 | 1982-02-24 | Yokohama Rubber Co Ltd:The | Epoxy resin composition |
| DE3811042A1 (de) | 1988-03-31 | 1989-10-19 | Merck Patent Gmbh | Ionenaustauscher |
| JPH0772233B2 (ja) * | 1991-02-19 | 1995-08-02 | 日本ゼオン株式会社 | エポキシ樹脂系発泡性組成物 |
| DE4317019A1 (de) * | 1992-05-27 | 1993-12-02 | Merck Patent Gmbh | Oberflächenmodifizierte Perlglanzpigmente |
| US5755486A (en) | 1995-05-23 | 1998-05-26 | Novamax Technologies Holdings, Inc. | Composite structural reinforcement member |
| JP3031272B2 (ja) * | 1996-12-05 | 2000-04-10 | 日本電気株式会社 | 樹脂組成物及びその成形体表面への導体形成方法 |
| EP0983312B1 (de) * | 1997-05-21 | 2002-09-25 | Denovus L.L.C. | Epoxyenthaltende schaumzusammensetzungen und dessen verwendung |
| US6387470B1 (en) | 1998-11-05 | 2002-05-14 | Sika Corporation | Sound deadening and structural reinforcement compositions and methods of using the same |
| DE19909270A1 (de) * | 1999-03-03 | 2000-09-07 | Henkel Teroson Gmbh | Hitzehärtbarer, thermisch expandierbarer Formkörper |
| FR2809741B1 (fr) | 2000-05-31 | 2002-08-16 | Atofina | Materiaux thermodurs a tenue au choc amelioree |
| DE10228228A1 (de) | 2001-09-14 | 2003-04-03 | Merck Patent Gmbh | Formkörper aus Kern-Mantel-Partikeln |
| CA2471368A1 (en) * | 2001-12-21 | 2003-07-03 | Henkel Teroson Gmbh | Expandable epoxy resin-based systems modified with thermoplastic polymers |
| US7119149B2 (en) * | 2003-01-03 | 2006-10-10 | Henkel Kommanditgesellschaft Auf | High expansion two-component structural foam |
| DE10327728A1 (de) | 2003-06-18 | 2005-01-27 | Sustech Gmbh & Co. Kg | Nanopartikuläres redispergierbares Zinkoxidpulver III |
| DE102004055303A1 (de) | 2004-11-16 | 2006-05-18 | Röhm GmbH & Co. KG | Kern-Mantel-Partikel |
| JP5091129B2 (ja) * | 2005-07-01 | 2012-12-05 | シーカ・テクノロジー・アーゲー | 固体熱膨張材料 |
| KR101303246B1 (ko) * | 2005-08-24 | 2013-09-06 | 헨켈 아일랜드 리미티드 | 개선된 내충격성을 갖는 에폭시 조성물 |
| DE102006048739A1 (de) | 2006-10-12 | 2008-04-17 | Henkel Kgaa | Expandierbare, thermisch härtbare Zusammensetzung auf Basis von Epoxidharzen mit verbesserten Fließeigenschaften |
| PL1867676T3 (pl) * | 2006-06-16 | 2011-08-31 | Sealants Europe Sas | Rozszerzalna kompozycja mastyksu do strukturalnego wzmacniania pustych w środku metalowych korpusów |
| EP1916270A1 (de) * | 2006-10-24 | 2008-04-30 | Sika Technology AG | Hitzehärtende Epoxidharzzusammensetzung mit blockiertem Polyurethanprepolymer |
| EP1916285A1 (de) * | 2006-10-24 | 2008-04-30 | Sika Technology AG | Derivatisiertes Epoxid-Festharz und dessen Verwendungen |
| DE102008053520A1 (de) * | 2008-10-28 | 2010-05-06 | Henkel Ag & Co. Kgaa | Strukturschaum auf Epoxidbasis mit thermoplastischen Polyurethanen |
-
2008
- 2008-10-28 DE DE102008053518A patent/DE102008053518A1/de not_active Withdrawn
-
2009
- 2009-09-23 KR KR1020117009605A patent/KR20110079687A/ko not_active Withdrawn
- 2009-09-23 BR BRPI0920077A patent/BRPI0920077A2/pt not_active IP Right Cessation
- 2009-09-23 EP EP09740074A patent/EP2350177B1/de not_active Not-in-force
- 2009-09-23 CN CN2009801424963A patent/CN102197070B/zh not_active Expired - Fee Related
- 2009-09-23 JP JP2011532558A patent/JP2012506918A/ja active Pending
- 2009-09-23 WO PCT/EP2009/062310 patent/WO2010049220A1/de not_active Ceased
- 2009-09-23 CA CA2741736A patent/CA2741736A1/en not_active Abandoned
- 2009-09-23 ES ES09740074T patent/ES2402757T3/es active Active
-
2011
- 2011-04-27 US US13/095,282 patent/US20110257285A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| EP2350177A1 (de) | 2011-08-03 |
| WO2010049220A1 (de) | 2010-05-06 |
| ES2402757T3 (es) | 2013-05-08 |
| JP2012506918A (ja) | 2012-03-22 |
| BRPI0920077A2 (pt) | 2016-04-05 |
| US20110257285A1 (en) | 2011-10-20 |
| CN102197070A (zh) | 2011-09-21 |
| EP2350177B1 (de) | 2013-01-23 |
| CN102197070B (zh) | 2013-04-24 |
| KR20110079687A (ko) | 2011-07-07 |
| DE102008053518A1 (de) | 2010-06-02 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EEER | Examination request |
Effective date: 20140922 |
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| FZDE | Discontinued |
Effective date: 20160923 |